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Recruiting NCT07685327

NCT07685327 Comparing Mixed Reality and Physical Therapy to Improve Balance and Coordination in Adolescents With Spastic Diplegic Cerebral Palsy

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Clinical Trial Summary
NCT ID NCT07685327
Status Recruiting
Phase —
Sponsor Ibadat International University, Islamabad
Condition Cerebral Palsy
Study Type INTERVENTIONAL
Enrollment 40 participants
Start Date 2026-01-12
Primary Completion 2026-07-01

Eligibility & Interventions

Sex All sexes
Min Age 10 Years
Max Age 19 Years
Study Type INTERVENTIONAL
Interventions
Meta Quest Pro Mixed Reality SystemStandard Physical Therapy

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 40 participants in total. It began in 2026-01-12 with a primary completion date of 2026-07-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This randomized controlled trial aims to compare the effectiveness of fully immersive Mixed Reality (MR) combined with standard physical therapy versus standard physical therapy alone in improving balance and coordination among adolescents with spastic diplegic cerebral palsy. A total of 40 participants aged 10 to 19 years will be randomly assigned to one of two treatment groups. The intervention will be provided three times per week for eight weeks. Balance and coordination will be assessed before treatment, at four weeks, and after completion of the intervention using validated clinical outcome measures. The findings of this study may help determine whether immersive Mixed Reality can enhance rehabilitation outcomes in adolescents with cerebral palsy.

Eligibility Criteria

Inclusion Criteria: * Male and female participants. * Adolescents aged 10 to 19 years. * Clinically diagnosed with spastic diplegic cerebral palsy. * Gross Motor Function Classification System (GMFCS) Levels I, II, or III. * Pediatric Balance Scale (PBS) score greater than 35. * Willing to participate in the study and provide written informed consent/assent with parental or legal guardian consent where applicable. Exclusion Criteria: * Cognitive impairment (MMSE score \<24). * History of seizure disorders. * Visual or hearing impairment that interferes with participation. * Diagnosed psychological or psychiatric disorders. * Any other medical condition that would prevent safe participation in the study.

Contact & Investigator

Central Contact

Muhammad Ashar Rafi, PhD*

✉ Ashar.rafi@uipt.iiui.edu.pk

📞 923083407837

Principal Investigator

Muhammad Yaseen Khattak, MS-PPT

PRINCIPAL INVESTIGATOR

Ibadat International University, Islamabad

Frequently Asked Questions

Who can join the NCT07685327 clinical trial?

This trial is open to participants of all sexes, aged 10 Years or older, up to 19 Years, studying Cerebral Palsy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07685327 currently recruiting?

Yes, NCT07685327 is actively recruiting participants. Contact the research team at Ashar.rafi@uipt.iiui.edu.pk for enrollment information.

Where is the NCT07685327 trial being conducted?

This trial is being conducted at Mansehra, Pakistan.

Who is sponsoring the NCT07685327 clinical trial?

NCT07685327 is sponsored by Ibadat International University, Islamabad. The principal investigator is Muhammad Yaseen Khattak, MS-PPT at Ibadat International University, Islamabad. The trial plans to enroll 40 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology